Roles of antiestrogen binding sites in human endometrial cancer cells |
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Authors: | M Hayashida N Terakawa I Shimizu H Ikegami H Wakimoto T Aono O Tanizawa K Matsumoto |
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Affiliation: | 1. Departments of Obstetrics and Gynecology,Osaka 553, Japan;2. Pathology, Osaka University Medical School, Osaka 553, Japan;1. Natural Products and Medicinal Chemistry Division, CSIR – Indian Institute of Integrative Medicine, Jammu 180001, India;2. Pharmacology Division, CSIR – Indian Institute of Integrative Medicine, Jammu 180001, India;3. Biotechnology Division, CSIR – Indian Institute of Integrative Medicine, Sanatnagar, Srinagar 190005, India;4. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India |
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Abstract: | Estrogen-noncompatible antiestrogen binding sites (AEBS) as well as estrogen receptors (ER), and the growth-inhibitory effect of tamoxifen were investigated in two human endometrial cancer cell lines, IK-90 and HEC-IA cells. IK-90 cells contained specific AEBS, but no ER was found in these cells. Scatchard plot analysis of AEBS in 12,000 g supernatant from IK-90 cells showed a high affinity binding site for tamoxifen (Kd:5.6 +/- 1.0 nM) with the maximum binding site of 457 +/- 47 fmol/mg protein. However, no measurable ER or AEBS was found in HEC-IA cells. The effect of tamoxifen on the growth of cells was found to be identical in both cell lines; the addition of 10 microM tamoxifen to culture medium was cytocidal whereas tamoxifen at lower concentrations (1 nM-1 microM) did not significantly affect the growth of both IK-90 and HEC-IA cells. These results demonstrate for the first time the presence of AEBS in human endometrial cancer cells. The present results also suggest that AEBS does not play a fundamental role in mediating the growth-inhibitory effect of tamoxifen in endometrial cancer cells. |
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